Variant report

Variant	rs72730365
Chromosome Location	chr4:151065311-151065312
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:151064651..151066657-chr4:151066791..151068654,2	MCF-7	breast:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10002193	0.85[ASN][1000 genomes]
rs10012983	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10857242	0.88[AFR][1000 genomes]
rs11099756	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11099757	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4129179	0.84[ASN][1000 genomes]
rs4240359	0.85[ASN][1000 genomes]
rs4411962	0.84[ASN][1000 genomes]
rs4513544	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6535713	0.84[ASN][1000 genomes]
rs72730355	0.88[AFR][1000 genomes]
rs72730358	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs72730387	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72730391	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72730393	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72732407	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7659245	0.84[ASN][1000 genomes]
rs7680670	0.84[ASN][1000 genomes]
rs9993737	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026797	chr4:150246932-151217137	Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv932022	chr4:150831733-151419552	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1032689	chr4:150971003-151316856	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv537300	chr4:150971003-151316856	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:151038800-151070000	Weak transcription	Ovary	ovary
2	chr4:151045200-151099000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:151049200-151074000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr4:151057800-151070600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:151061800-151069800	Weak transcription	Left Ventricle	heart
6	chr4:151061800-151071800	Weak transcription	Brain Anterior Caudate	brain
7	chr4:151062800-151066800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:151062800-151067000	Weak transcription	HMEC	breast
9	chr4:151062800-151071800	Weak transcription	Colon Smooth Muscle	Colon
10	chr4:151062800-151072000	Weak transcription	Aorta	Aorta
11	chr4:151063000-151066000	Weak transcription	Osteobl	bone
12	chr4:151063000-151066400	Weak transcription	NH-A	brain
13	chr4:151063000-151066600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr4:151063000-151070800	Weak transcription	HSMMtube	muscle
15	chr4:151063200-151066400	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr4:151063200-151066400	Weak transcription	NHLF	lung
17	chr4:151063200-151066600	Weak transcription	NHEK	skin
18	chr4:151063200-151067200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:151063200-151070600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:151063400-151066400	Weak transcription	NHDF-Ad	bronchial
21	chr4:151063400-151066600	Weak transcription	HSMM	muscle
22	chr4:151063400-151070600	Weak transcription	Fetal Heart	heart
23	chr4:151063600-151066400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:151063600-151066400	Weak transcription	Hela-S3	cervix
25	chr4:151063600-151066800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:151063600-151070200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr4:151064400-151066400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:151064400-151066800	Weak transcription	Fetal Lung	lung
29	chr4:151064600-151080200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:151065200-151066400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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